Wheelchair use in genetically confirmed FSHD1 from a large cohort study in Chinese population-Reference-Cited by-同舟云学术

Wheelchair use in genetically confirmed FSHD1 from a large cohort study in Chinese population

Published:2022-03-18 Issue:6 Volume:145 Page:e51-e54
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:

Author:

Qiu Liangliang¹,Chen Long¹,Zheng Fuze¹,Lin Minting¹,Lin Yi¹,Fu Ying¹^ORCID,Wang Ning¹,Wang Zhiqiang¹^ORCID

Affiliation:

1. Department of Neurology and Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University , Fuzhou 350005 , China

Funder

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awac097/43780751/awac097.pdf

Reference6 articles.

1. Predictors of functional outcomes in patients with facioscapulohumeral muscular dystrophy;Katz;Brain,2021

2. Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study;Wang;Lancet Reg Health West Pac,2021

3. Improving the assessment of outcomes in stroke: use of a structured interview to assign grades on the modified Rankin Scale;Wilson;Stroke,2002

4. Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype;Ricci;Ann Neurol,1999

5. Clinical and genetic features of somatic mosaicism in facioscapulohumeral dystrophy;Qiu;J Med Genet,2020

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Quantifying anti-DUX4 therapy for facioscapulohumeral muscular dystrophy;2024-08-15

2. Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy;Neurology;2023-07-18

3. An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 1;Brain;2023-06-23

4. Reply: Wheelchair use in genetically confirmed FSHD1 from a large cohort study in Chinese population;Brain;2022-03-18